Hall BD - Search Results

1

Penoscrotal transposition and associated anomalies: report of five new cases and review of the literature.

Parida SK, Hall BD, Barton L, Fujimoto A. Parida SK, et al. Among authors: hall bd. Am J Med Genet. 1995 Oct 23;59(1):68-75. doi: 10.1002/ajmg.1320590115. Am J Med Genet. 1995. PMID: 8849015 Review.

2

Hiatus/paraesophageal hernias in neonatal Marfan syndrome.

Parida SK, Kriss VM, Hall BD. Parida SK, et al. Among authors: hall bd. Am J Med Genet. 1997 Oct 17;72(2):156-8. doi: 10.1002/(sici)1096-8628(19971017)72:2<156::aid-ajmg6>3.0.co;2-t. Am J Med Genet. 1997. PMID: 9382135

3

Neonatal progeroid (Wiedemann-Rautenstrauch) syndrome: report of five new cases and review.

Pivnick EK, Angle B, Kaufman RA, Hall BD, Pitukcheewanont P, Hersh JH, Fowlkes JL, Sanders LP, O'Brien JM, Carroll GS, Gunther WM, Morrow HG, Burghen GA, Ward JC. Pivnick EK, et al. Among authors: hall bd. Am J Med Genet. 2000 Jan 17;90(2):131-40. Am J Med Genet. 2000. PMID: 10607952 Review.

4

Beare-Stevenson cutis gyrata syndrome.

Hall BD, Cadle RG, Golabi M, Morris CA, Cohen MM Jr. Hall BD, et al. Am J Med Genet. 1992 Sep 1;44(1):82-9. doi: 10.1002/ajmg.1320440120. Am J Med Genet. 1992. PMID: 1519658

5

Vascular abnormalities at the site of limb deficiency.

Hall BD. Hall BD. Am J Med Genet. 1992 Jun 1;43(3):619-20. doi: 10.1002/ajmg.1320430323. Am J Med Genet. 1992. PMID: 1605260

6

Diastrophic dysplasia: extreme variability within a sibship.

Hall BD. Hall BD. Am J Med Genet. 1996 May 3;63(1):28-33. doi: 10.1002/(SICI)1096-8628(19960503)63:1<28::AID-AJMG8>3.0.CO;2-O. Am J Med Genet. 1996. PMID: 8723083

7

Expanded phenotype and ethnicity in Setleis syndrome.

Clark RD, Golabi M, Lacassie Y, Hall B, Seto S. Clark RD, et al. Am J Med Genet. 1989 Nov;34(3):354-7. doi: 10.1002/ajmg.1320340311. Am J Med Genet. 1989. PMID: 2596524

8

Neurosonographic diagnosis of thalamic/basal ganglia vasculopathy in trisomy 13--an important diagnostic aid.

Chabra S, Kriss VM, Pauly TH, Hall BD. Chabra S, et al. Among authors: hall bd. Am J Med Genet. 1997 Oct 31;72(3):291-3. doi: 10.1002/(sici)1096-8628(19971031)72:3<291::aid-ajmg7>3.0.co;2-u. Am J Med Genet. 1997. PMID: 9332656

9

Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL): clinical and radiological findings in a Guatemalan patient.

Bradburn JM, Hall BD. Bradburn JM, et al. Among authors: hall bd. Am J Med Genet. 1995 Nov 6;59(2):234-7. doi: 10.1002/ajmg.1320590222. Am J Med Genet. 1995. PMID: 8588592

10

Nager acrofacial dysostosis: autosomal dominant inheritance in mild to moderately affected mother and lethally affected phocomelic son.

Hall BD. Hall BD. Am J Med Genet. 1989 Jul;33(3):394-7. doi: 10.1002/ajmg.1320330321. Am J Med Genet. 1989. PMID: 2801774

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